Philips recalls SENSE Breast Coil 3.0T 7ch MRI coils due to potential patient harm during scans. Affected units have specific serial numbers and reference codes.
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Philips is recalling its SENSE Breast Coil 3.0T 7ch MRI coils because they could harm patients during scans. This recall affects people using these coils for breast imaging.
The coil may cause harm during preparation or the scan itself. This could happen if the coil is not properly secured or if there are issues with the scanning process.
Patients undergoing breast MRI scans with the recalled coil model are most at risk. The recall applies to specific serial numbers and reference codes.
Check for the serial numbers 16, 7, 22, or 52 on the coil. The reference code 453530089302 and UDI-DI 00884838065413 also identify affected units.
Look for the serial numbers 16, 7, 22, or 52 on the coil.
The recalled model is Philips SENSE Breast Coil 3.0T 7ch.
Check for serial numbers 16, 7, 22, or 52 on the coil. The reference code 453530089302 and UDI-DI 00884838065413 also identify affected units.
The recall record does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0546-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-0546-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
